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Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
|
pubmed:dateCreated |
1982-8-14
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:status |
MEDLINE
|
pubmed:month |
Jun
|
pubmed:issn |
0007-1048
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
51
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
333-4
|
pubmed:dateRevised |
2004-11-17
|
pubmed:meshHeading |
pubmed-meshheading:7082589-Adult,
pubmed-meshheading:7082589-Aged,
pubmed-meshheading:7082589-Chromosome Aberrations,
pubmed-meshheading:7082589-Chromosome Disorders,
pubmed-meshheading:7082589-Female,
pubmed-meshheading:7082589-Hemoglobinuria, Paroxysmal,
pubmed-meshheading:7082589-Humans,
pubmed-meshheading:7082589-Karyotyping,
pubmed-meshheading:7082589-Male,
pubmed-meshheading:7082589-Middle Aged
|
pubmed:year |
1982
|
pubmed:articleTitle |
Normal karyotype in seven patients with paroxysmal nocturnal haemoglobinuria.
|
pubmed:publicationType |
Letter
|